ENST00000706952.1:c.3149T>A
|
ENSP00000516672.1:p.Val1050Asp
|
|
ENST00000638521.1:c.942T>A
|
|
|
ENST00000638869.1:c.451T>A
|
|
|
ENST00000639642.1:c.280T>A
|
|
|
ENST00000640005.1:c.53T>A
|
ENSP00000491293.1:p.Val18Asp
|
|
ENST00000640694.1:c.2990T>A
|
ENSP00000492403.1:p.Val997Asp
|
|
ENST00000642864.1:c.2990T>A
MANE Select
|
ENSP00000495726.1:p.Val997Asp
|
|
ENST00000674510.1:c.2990T>A
|
ENSP00000502054.1:p.Val997Asp
|
|
ENST00000674761.1:n.1297T>A
|
|
|
ENST00000675719.1:c.2960T>A
|
ENSP00000501927.1:p.Val987Asp
|
|
ENST00000375365.2:c.2375T>A
|
ENSP00000364514.2:p.Val792Asp
|
|
ENST00000396435.7:c.2990T>A
|
ENSP00000379712.3:p.Val997Asp
|
|
NM_001111125.2:c.2990T>A
|
NP_001104595.1:p.Val997Asp
|
|
NM_015075.1:c.2375T>A
|
NP_055890.1:p.Val792Asp
|
|
XM_006724579.2:c.3086T>A
|
XP_006724642.1:p.Val1029Asp
|
|
XM_006724580.2:c.2375T>A
|
XP_006724643.1:p.Val792Asp
|
|
XM_006724581.2:c.3086T>A
|
XP_006724644.1:p.Val1029Asp
|
|
XM_006724582.2:c.3086T>A
|
XP_006724645.1:p.Val1029Asp
|
|
XM_006724583.2:c.3086T>A
|
XP_006724646.1:p.Val1029Asp
|
|
XM_006724584.2:c.3086T>A
|
XP_006724647.1:p.Val1029Asp
|
|
XM_011530772.1:c.2312T>A
|
XP_011529074.1:p.Val771Asp
|
|
XM_011530773.1:c.2279T>A
|
XP_011529075.1:p.Val760Asp
|
|
XM_011530774.1:c.3086T>A
|
XP_011529076.1:p.Val1029Asp
|
|
XM_011530775.1:c.3086T>A
|
XP_011529077.1:p.Val1029Asp
|
|
XM_011530776.1:c.3086T>A
|
XP_011529078.1:p.Val1029Asp
|
|
XM_011530777.1:c.3086T>A
|
XP_011529079.1:p.Val1029Asp
|
|
XR_938365.1:n.3313T>A
|
|
|
XM_006724579.3:c.3086T>A
|
XP_006724642.1:p.Val1029Asp
|
|
XM_006724580.3:c.2375T>A
|
XP_006724643.1:p.Val792Asp
|
|
XM_006724581.4:c.3086T>A
|
XP_006724644.1:p.Val1029Asp
|
|
XM_006724582.4:c.3086T>A
|
XP_006724645.1:p.Val1029Asp
|
|
XM_006724583.4:c.3086T>A
|
XP_006724646.1:p.Val1029Asp
|
|
XM_006724584.3:c.3086T>A
|
XP_006724647.1:p.Val1029Asp
|
|
XM_011530773.2:c.2279T>A
|
XP_011529075.1:p.Val760Asp
|
|
XM_011530774.3:c.3086T>A
|
XP_011529076.1:p.Val1029Asp
|
|
XM_011530776.2:c.3086T>A
|
XP_011529078.1:p.Val1029Asp
|
|
XM_011530777.2:c.3086T>A
|
XP_011529079.1:p.Val1029Asp
|
|
XM_017029359.2:c.2960T>A
|
XP_016884848.1:p.Val987Asp
|
|
XM_017029360.1:c.2492T>A
|
XP_016884849.1:p.Val831Asp
|
|
XR_938365.2:n.3307T>A
|
|
|
NM_001111125.3:c.2990T>A
MANE Select
|
NP_001104595.1:p.Val997Asp
|
|
NM_015075.2:c.2375T>A
|
NP_055890.1:p.Val792Asp
|
|